1. Adelaide Research & Scholarship

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Results 31-40 of 45 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2012Common variants at 6q22 and 17q21 are associated with intracranial volumeIkram, M.; Fornage, M.; Smith, A.; Seshadri, S.; Schmidt, R.; Debette, S.; Vrooman, H.; Sigurdsson, S.; Ropele, S.; Taal, H.; Mook-Kanamori, D.; Coker, L.; Longstreth Jr, W.; Niessen, W.; DeStefano, A.; Beiser, A.; Zijdenbos, A.; Struchalin, M.; Jack Jr, C.; Rivadeneira, F.; et al.
2011Association of genetic loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 childrenBarker, A.; Sharp, S.; Timpson, N.; Bouatia-Naji, N.; Warrington, N.; Kanoni, S.; Beilin, L.; Brage, S.; Deloukas, P.; Evans, D.; Grontved, A.; Hassanali, N.; Lawlor, D.; Lecoeur, C.; Loos, R.; Lye, S.; McCarthy, M.; Mori, T.; Coumba Ndiaye, N.; Newnham, J.; et al.
2010Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distributionHeid, I.; Jackson, A.; Randall, J.; Winkler, T.; Qi, L.; Steinthorsdottir, V.; Thorleifsson, G.; Zillikens, M.; Speliotes, E.; Magi, R.; Workalemahu, T.; White, C.; Bouatia-Naji, N.; Harris, T.; Berndt, S.; Ingelsson, E.; Willer, C.; Weedon, M.; Luan, J.; Vedantam, S.; et al.
2011Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesStrawbridge, R.; Dupuis, J.; Prokopenko, I.; Barker, A.; Ahlqvist, E.; Rybin, D.; Petrie, J.; Travers, M.; Bouatia-Naji, N.; Dimas, A.; Nica, A.; Wheeler, E.; Chen, H.; Voight, B.; Taneera, J.; Kanoni, S.; Peden, J.; Turrini, F.; Gustafsson, S.; Zabena, C.; et al.
2011A genome-wide significant linkage for severe depression on chromosome 3: the depression network studyBreen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.
2008Identifying genetic traces of historical expansions: Phoenician footprints in the MediterraneanZalloua, P.; Platt, D.; El Sibai, M.; Khalife, J.; Makhoul, N.; Haber, M.; Xue, Y.; Izaabel, H.; Bosch, E.; Adams, S.; Arroyo, E.; Lopez-Parra, A.; Aler, M.; Picornell, A.; Ramon, M.; Jobling, M.; Comas, D.; Bertranpetit, J.; Spencer Wells, R.; Tyler-Smith, C.; et al.; Cooper, Alan
2008Y-chromosomal diversity in Lebanon is structured by recent historical eventsZalloua, P.; Xue, Y.; Khalife, J.; Makhoul, N.; Debiane, L.; Platt, D.; Royyuru, A.; Herrera, R.; Hernanz, D.; Blue-Smith, J.; Spencer Wells, R.; Comas, D.; Bertranpetit, J.; Tyler-Smith, C.; Schurr, T.; Santos, F.; Quintana-Murci, L.; Balanovska, E.; Balanovsky, O.; Behar, D.; et al.; Cooper, Alan
2011Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.
2011Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaHahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.
2015A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adultsPerez-Andreu, V.; Roberts, K.; Xu, H.; Smith, C.; Zhang, H.; Yang, W.; Harvey, R.; Payne-Turner, D.; Devidas, M.; Cheng, I.; Carroll, W.; Heerema, N.; Carroll, A.; Raetz, E.; Gastier-Foster, J.; Marcucci, G.; Bloomfield, C.; Mrozek, K.; Kohlschmidt, J.; Stock, W.; et al.

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